Fluoxetine - 0093-1042-93 - (Fluoxetine)

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Drug Information of Fluoxetine

Product NDC: 0093-1042
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine
Active Ingredient(s): 10    mg/1 & nbsp;   Fluoxetine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 0093-1042
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075452
Marketing Category: ANDA
Start Marketing Date: 20020130

Package Information of Fluoxetine

Package NDC: 0093-1042-93
Package Description: 100 BLISTER PACK in 1 BOX (0093-1042-93) > 1 CAPSULE in 1 BLISTER PACK (0093-1042-19)

NDC Information of Fluoxetine

NDC Code 0093-1042-93
Proprietary Name Fluoxetine
Package Description 100 BLISTER PACK in 1 BOX (0093-1042-93) > 1 CAPSULE in 1 BLISTER PACK (0093-1042-19)
Product NDC 0093-1042
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20020130
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine


General Information